Canonical Allele Identifier: CA406291680

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs909824341
• MyVariant Identifiers: chr19:g.45451757G>A (hg19) ; chr19:g.44948500G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948500G>A , CM000681.2:g.44948500G>A	GRCh38
NC_000019.9:g.45451757G>A , CM000681.1:g.45451757G>A	GRCh37
NC_000019.8:g.50143597G>A	NCBI36
NG_008837.1:g.7515G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.22G>A (APOC2) MANE Select	ENSP00000252490.5:p.Ala8Thr
ENST00000252490.5:c.22G>A (APOC4-APOC2)	ENSP00000252490.4:p.Ala8Thr
ENST00000585685.5:c.*805G>A (APOC4-APOC2)	ENSP00000467185.1:n.*805G>A
ENST00000585786.1:c.22G>A (APOC2)	ENSP00000465001.1:p.Ala8Thr
ENST00000589057.5:c.253G>A (APOC4-APOC2)	ENSP00000468139.1:p.Ala85Thr
ENST00000590360.2:c.22G>A (APOC2)	ENSP00000466775.1:p.Ala8Thr
ENST00000591597.5:c.22G>A (APOC2)	ENSP00000476835.1:p.Ala8Thr
ENST00000592257.5:c.22G>A (APOC2)	ENSP00000477261.1:p.Ala8Thr
NM_000483.4:c.22G>A (APOC2)	NP_000474.2:p.Ala8Thr
NR_037932.1:n.1229G>A (APOC4-APOC2)
NM_000483.5:c.22G>A (APOC2) MANE Select	NP_000474.2:p.Ala8Thr